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Phosphonous Dichloride, (2-Chloro-1,1-Dimethylethyl)- (8Ci,9Ci)

    • Product Name Phosphonous Dichloride, (2-Chloro-1,1-Dimethylethyl)- (8Ci,9Ci)
    • Alias tert-Butylphosphonic dichloride
    • Einecs 247-431-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    139562

    Cas Number 598-95-4
    Molecular Formula C4H9Cl3P
    Molecular Weight 211.44
    Iupac Name 2-chloro-1,1-dimethylethylphosphonous dichloride
    Synonyms tert-Butylphosphonous dichloride, (2-Chloro-1,1-dimethylethyl)phosphonous dichloride
    Appearance Colorless to pale yellow liquid
    Boiling Point 57-59°C at 15 mmHg
    Density 1.29 g/cm³
    Solubility Reacts with water

    As an accredited Phosphonous Dichloride, (2-Chloro-1,1-Dimethylethyl)- (8Ci,9Ci) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 mL sealed amber glass bottle with tamper-evident cap, labeled with hazard symbols, product name, and handling precautions.
    Shipping **Shipping Description:** Phosphonous Dichloride, (2-Chloro-1,1-Dimethylethyl)- (8Ci,9Ci) should be shipped in tightly sealed, corrosion-resistant containers, labeled as a toxic and moisture-sensitive chemical. Use appropriate hazardous materials packaging, with UN-approved labeling for toxic inorganic substances. Transport according to local, national, and international hazardous goods regulations. Store upright, away from heat or water sources.
    Storage **Phosphonous Dichloride, (2-Chloro-1,1-Dimethylethyl)- (8Ci,9Ci)** should be stored in a cool, dry, well-ventilated area away from moisture and incompatible substances such as strong oxidizers and bases. Keep container tightly closed in a chemical-resistant, clearly labeled bottle. Protect from direct sunlight, heat, and ignition sources. Use appropriate secondary containment and ensure access to emergency spill procedures.
    Application of Phosphonous Dichloride, (2-Chloro-1,1-Dimethylethyl)- (8Ci,9Ci)

    Applications of Phosphonous Dichloride, (2-Chloro-1,1-Dimethylethyl)- (8Ci,9Ci) in Industrial Manufacturing

    As a dedicated producer of Phosphonous Dichloride, (2-Chloro-1,1-Dimethylethyl)- (8Ci,9Ci), we support a range of downstream sectors that rely on this intermediate for precise technical requirements. Below, we detail its practical roles in key industries where our material delivers consistency and reliability throughout scale-up and ongoing manufacturing.

    1. Synthesis of Organophosphorus Agrochemical Active Ingredients

    Manufacturers engaged in crop protection formulation utilize this compound as a key chlorinating and phosphorylating agent for developing modern organophosphorus pesticide precursors. Integration at the early intermediate stage enables precise control over purity and reaction efficiency in high-throughput syntheses, directly impacting the standardization of downstream actives.

    Industry compliance standards

    • FAO/WHO Guidelines for Active Ingredient Purity
    • ISO 9001:2015 Quality Management for Chemicals
    • REACH Registration for Agrochemical Intermediates
    • National Environmental Regulations for Pesticide Manufacturing (e.g., US EPA, EU BPR)

    Typical usage ratio

    • 3%–7% w/w in intermediate synthesis steps, adjusted per batch scale and stoichiometry of the targeted phosphorus compound

    Downstream process integration

    • Introduced during controlled chlorination of substituted phosphines or phosphites, followed by coupling or further functionalization prior to formulation blending

    Final product types

    • Organophosphorus insecticide intermediates (e.g., for chlorpyrifos synthesis)
    • Herbicide precursors
    • Specialty fungicide building blocks
    • Regulatory-approved agrochemical actives for export markets

    2. Flame Retardant Additive Precursors in Engineering Plastics

    Producers of flame-resistant polymers select this intermediate to manufacture phosphinate- and phosphonate-based additives. Its high reactivity ensures efficient incorporation of phosphorus moieties, facilitating downstream processes where melt-compounding and resin modification for enhanced fire safety performance are critical prior to end-use certification.

    Industry compliance standards

    • UL94 Flammability Testing (Resins, End Products)
    • RoHS & REACH for Additive Chemicals
    • ISO 1043-4: Plastics — Symbols — Flame Retardants
    • EN 45545-2 (Fire Protection for Railway Rolling Stock)

    Typical usage ratio

    • 2%–10% relative to monomer mass in phosphorus additive synthesis; final active loading in compound governed by polymer type and flammability class

    Downstream process integration

    • Added during phosphorus additive manufacture by chlorination/esterification, filtered and dried prior to compounding into polyamide, ABS, or polycarbonate melts via twin-screw extrusion

    Final product types

    • High-performance flame retardant masterbatches
    • Polymer resins for electronics housing
    • Automotive interior components
    • Electrical insulation sheathing

    3. Pharmaceutical Intermediate for Organophosphorus Drug Synthesis

    API manufacturers source this compound for tightly controlled cyclization and phosphorylation reactions when preparing certain organophosphorus drug precursors. Strict process control ensures compliance with trace impurity limits and supports high reproducibility in multi-step synthesis environments governed by cGMP standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidelines
    • USP and Ph. Eur. monographs (where applicable)
    • FDA CFR Part 211 (for US-bound APIs)
    • ISO 13485 (for device-related pharmaceutical intermediates)

    Typical usage ratio

    • 0.5%–3% in phosphorylation steps; molar dosage determined by desired yield and required residual control per batch protocol

    Downstream process integration

    • Charged in closed-reactor vessel for condensation or cyclization, typically following solvent pre-charge and auxiliary base addition, with real-time in-process monitoring for batch standardization

    Final product types

    • Chiral phosphorus-based pharmaceutical intermediates
    • Central nervous system agent precursors
    • Antiviral prodrug building blocks
    • Contract-manufactured small molecule intermediates for global-brand pharmaceuticals

    4. Ligand Preparation in Organometallic Catalysis Manufacturing

    Fine chemical and catalyst producers employ this intermediate to functionalize ligands for transition metal coordination catalysts. The compound supplies the reactive phosphorus unit in site-specific ligand design, supporting downstream catalyst complexation and ensuring the required purity and reactivity in homogeneous or supported catalyst systems.

    Industry compliance standards

    • ISO 9001/14001 Integrated Management Systems
    • SHE/Process Safety Rules (e.g., Responsible Care, Seveso Directive)
    • Specialty Chemical Substance Registration (e.g., TSCA, REACH)
    • Custom specification agreements for high-purity reagents

    Typical usage ratio

    • 1–5 mol% relative to target ligand backbone; tailored to the design of the complexation site and required catalytic activity

    Downstream process integration

    • Introduced at the organophosphorus functionalization stage, typically in inert-atmosphere batch or continuous flow reactors, followed by extraction, crystallization, and purity validation

    Final product types

    • P-ligand complexes for cross-coupling catalysts
    • Homogeneous hydrogenation catalyst precursors
    • Chiral phosphine ligands for enantioselective synthesis
    • Customized catalysts supplied to fine chemical and pharmaceutical manufacturers

    5. Advanced Surface Modification for Specialty Coatings

    Producers of high-durability coatings and surface treatment agents utilize the compound as a precursor for synthesizing functional phosphonate or phosphinate esters. The application ensures reliable anchoring of phosphorus groups, thus supporting specialty coatings with enhanced corrosion resistance, especially in steel and aluminum substrate applications where alternative surface chemistry cannot meet the environmental or performance criteria.

    Industry compliance standards

    • ISO 12944 (Corrosion Protection by Paint Systems)
    • ASTM D3359 Adhesion Testing
    • REACH Annex XVII — Restriction of Hazardous Substances in Coatings
    • OEM Automotive Surface Coating Standards (e.g., Daimler DBL 7381)

    Typical usage ratio

    • 5%–12% w/w in initial ester synthesis; subsequent surface treatment loading adjusted based on targeted substrate coverage and thickness specifications

    Downstream process integration

    • Participates in transesterification or substitution at the monomer preparation stage, with formulation completed before downstream spray, dip, or roll-application onto metal substrates in line with cure schedules

    Final product types

    • Corrosion-resistant primer systems
    • Electrostatic powder coatings with phosphorus-functional groups
    • Protective phosphate conversion surface treatments
    • Heavy-duty marine and automotive coatings
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